These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
117 related articles for article (PubMed ID: 36039657)
1. GP2017-HCF, a high concentration formulation, demonstrates similar pharmacokinetics, immunogenicity and safety to GP2017, an approved adalimumab biosimilar. von Richter O; O'Reilly T; Guerrieri D; Fan J; Fey C; Schussler S; Furlan F; Lemke L Expert Opin Biol Ther; 2023; 23(8):749-758. PubMed ID: 36039657 [TBL] [Abstract][Full Text] [Related]
2. Differences in immunogenicity associated with non-product related variability: insights from two pharmacokinetic studies using GP2017, an adalimumab biosimilar. von Richter O; Lemke L; Haliduola H; Balfour A; Zehnpfennig B; Skerjanec A; Jauch-Lembach J Expert Opin Biol Ther; 2019 Oct; 19(10):1057-1064. PubMed ID: 31002537 [No Abstract] [Full Text] [Related]
3. GP2017, an adalimumab biosimilar: pharmacokinetic similarity to its reference medicine and pharmacokinetics comparison of different administration methods. von Richter O; Lemke L; Haliduola H; Fuhr R; Koernicke T; Schuck E; Velinova M; Skerjanec A; Poetzl J; Jauch-Lembach J Expert Opin Biol Ther; 2019 Oct; 19(10):1075-1083. PubMed ID: 30698045 [No Abstract] [Full Text] [Related]
4. 'Totality of Evidence' Approach in the Development of GP2017, an Approved Adalimumab Biosimilar. Gaylis N; Both C; Lemke L; von Richter O; Yamauchi P Adv Ther; 2024 May; 41(5):1795-1814. PubMed ID: 38514505 [TBL] [Abstract][Full Text] [Related]
5. Pharmacokinetic equivalence, comparable safety, and immunogenicity of an adalimumab biosimilar product (M923) to Humira in healthy subjects. Hillson J; Mant T; Rosano M; Huntenburg C; Alai-Safar M; Darne S; Palmer D; Pavlova BG; Doralt J; Reeve R; Goel N; Weilert D; Rhyne PW; Chance K; Caminis J; Roach J; Ganguly T Pharmacol Res Perspect; 2018 Feb; 6(1):. PubMed ID: 29417761 [TBL] [Abstract][Full Text] [Related]
6. Pharmacokinetics and safety of candidate tocilizumab biosimilar CT-P47 versus reference tocilizumab: a randomized, double-blind, single-dose phase I study. Yu KS; Kim B; Shin D; Park MK; Hwang JG; Kim MG; Chung H; Ghim J; Chung JY; Smolen JS; Burmester GR; Kim S; Bae Y; Jeon D; Yoo J; Yang G; Bae J; Keystone E Expert Opin Investig Drugs; 2023 May; 32(5):429-439. PubMed ID: 37231670 [TBL] [Abstract][Full Text] [Related]
7. A Randomized Pharmacokinetic Study in Healthy Male Subjects Comparing a High-concentration, Citrate-free SB5 Formulation (40 mg/0.4 ml) and Prior SB5 (Adalimumab Biosimilar). Ahn SS; Lee M; Baek Y; Lee S Rheumatol Ther; 2022 Aug; 9(4):1157-1169. PubMed ID: 35776269 [TBL] [Abstract][Full Text] [Related]
8. Pharmacokinetics, safety, and immunogenicity of HLX03, an adalimumab biosimilar, compared with reference biologic in healthy Chinese male volunteers: Results of a randomized, double-blind, parallel-controlled, phase 1 study. Zhang H; Wu M; Sun J; Zhu X; Li C; Ding Y; Zhang X; Chai K; Li X Pharmacol Res Perspect; 2021 Apr; 9(2):e00733. PubMed ID: 33682358 [TBL] [Abstract][Full Text] [Related]
9. Signal-to-noise ratio to assess magnitude, kinetics and impact on pharmacokinetics of the immune response to an adalimumab biosimilar. Guerrieri D; Horvat M; Fan J; Wang J; Lemke L; Richter OV; Poetzl J Bioanalysis; 2024 Jan; 16(1):33-48. PubMed ID: 38031738 [No Abstract] [Full Text] [Related]
10. A plain language summary describing how two different concentrations of GP2017, a biosimilar adalimumab medicine, are associated with similar drug levels within the body. Danese S; Wiland P; Cohen R; Gaylis N; Both C; Jathanakodi S; Fey C; Lemke L; Blauvelt A Immunotherapy; 2023 Dec; 15(18):1501-1509. PubMed ID: 38031712 [TBL] [Abstract][Full Text] [Related]
11. Comparison of pharmacokinetics, pharmacodynamics, safety, and immunogenicity of teriparatide biosimilar with EU- and US-approved teriparatide reference products in healthy men and postmenopausal women. Fenwick S; Vekariya V; Patel R; Hajela P; Modi K; Kale P; Nath A Osteoporos Int; 2023 Jan; 34(1):179-188. PubMed ID: 36287230 [TBL] [Abstract][Full Text] [Related]
12. A randomized trial comparing LY01011, biosimilar candidate, with the reference product denosumab (Xgeva®) in healthy Chinese subjects. Ding Y; Liu Y; Dou C; Guo S J Bone Oncol; 2023 Oct; 42():100499. PubMed ID: 37701913 [TBL] [Abstract][Full Text] [Related]
13. Randomised, phase I pharmacokinetic study of adalimumab biosimilar CT-P17 (40 mg/0.4 mL) by autoinjector and prefilled syringe in healthy subjects. Davidson A; Brimhall D; Kay J; Keystone E; Lee SJ; Kim SH; Bae YJ; Choi EJ; Furst DE Br J Clin Pharmacol; 2021 Nov; 87(11):4323-4333. PubMed ID: 33822406 [TBL] [Abstract][Full Text] [Related]
14. Bioequivalence, safety and immunogenicity of BI 695501, an adalimumab biosimilar candidate, compared with the reference biologic in a randomized, double-blind, active comparator phase I clinical study (VOLTAIRE®-PK) in healthy subjects. Wynne C; Altendorfer M; Sonderegger I; Gheyle L; Ellis-Pegler R; Buschke S; Lang B; Assudani D; Athalye S; Czeloth N Expert Opin Investig Drugs; 2016 Dec; 25(12):1361-1370. PubMed ID: 27813422 [TBL] [Abstract][Full Text] [Related]
15. Pharmacokinetics, safety, tolerability and immunogenicity of FKB327, a new biosimilar medicine of adalimumab/Humira, in healthy subjects. Puri A; Niewiarowski A; Arai Y; Nomura H; Baird M; Dalrymple I; Warrington S; Boyce M Br J Clin Pharmacol; 2017 Jul; 83(7):1405-1415. PubMed ID: 28133772 [TBL] [Abstract][Full Text] [Related]
16. A randomized, double-blind, single-dose, two-arm, parallel study comparing pharmacokinetics, immunogenicity and tolerability of branded adalimumab and its biosimilar LBAL in healthy male volunteers. Park KR; Chung H; Yang SM; Lee S; Yoon SH; Cho JY; Jang IJ; Yu KS Expert Opin Investig Drugs; 2017 May; 26(5):619-624. PubMed ID: 28290731 [TBL] [Abstract][Full Text] [Related]
17. Relative bioavailability, immunogenicity, and safety of two adalimumab-adbm formulations in healthy volunteers: a double-blind, randomized, single-dose, parallel-arm Phase I trial (VOLTAIRE-HCLF). Moschetti V; Buschke S; Bertulis J; Hohl K; McCabe D Expert Opin Biol Ther; 2024 Jul; 24(7):673-679. PubMed ID: 38739422 [TBL] [Abstract][Full Text] [Related]
18. Phase I, randomized, double-blind, single-dose study to assess the pharmacokinetics, safety, and immunogenicity of the proposed biosimilar SCT630 and adalimumab in healthy Chinese subjects. Liu L; Qi L; Lei C; Wang Y; Zhang W; Liu Y; Li P; Bai H; Li Y; Li Y; Liu J; Xie L; Wang X Int Immunopharmacol; 2022 May; 106():108599. PubMed ID: 35193054 [TBL] [Abstract][Full Text] [Related]
19. Phase III randomized study of the proposed adalimumab biosimilar GP2017 in psoriasis: impact of multiple switches. Blauvelt A; Lacour JP; Fowler JF; Weinberg JM; Gospodinov D; Schuck E; Jauch-Lembach J; Balfour A; Leonardi CL Br J Dermatol; 2018 Sep; 179(3):623-631. PubMed ID: 29917226 [TBL] [Abstract][Full Text] [Related]
20. A randomized, double-blind, 3-arm, parallel study assessing the pharmacokinetics, safety, tolerability and immunogenicity of AVT04, an ustekinumab candidate biosimilar, in healthy adults. Wynne C; Hamilton P; McLendon K; Stroissnig H; Smith M; Duijzings P; Ruffieux R; Otto H; Sattar A; Haliduola HN; Leutz S; Berti F Expert Opin Investig Drugs; 2023 May; 32(5):417-427. PubMed ID: 37212315 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]